These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

139 related articles for article (PubMed ID: 26240990)

  • 21. Association between early-onset Parkinson's disease and mutations in the parkin gene.
    Lücking CB; Dürr A; Bonifati V; Vaughan J; De Michele G; Gasser T; Harhangi BS; Meco G; Denèfle P; Wood NW; Agid Y; Brice A; ;
    N Engl J Med; 2000 May; 342(21):1560-7. PubMed ID: 10824074
    [TBL] [Abstract][Full Text] [Related]  

  • 22. parkin mutation analysis in clinic patients with early-onset Parkinson [corrected] disease.
    Poorkaj P; Nutt JG; James D; Gancher S; Bird TD; Steinbart E; Schellenberg GD; Payami H
    Am J Med Genet A; 2004 Aug; 129A(1):44-50. PubMed ID: 15266615
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Molecular analysis of the parkin gene in South African patients diagnosed with Parkinson's disease.
    Bardien S; Keyser R; Yako Y; Lombard D; Carr J
    Parkinsonism Relat Disord; 2009 Feb; 15(2):116-21. PubMed ID: 18514563
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Mutation analysis of parkin and PINK1 genes in early-onset Parkinson's disease in China.
    Zhang BR; Hu ZX; Yin XZ; Cai M; Zhao GH; Liu ZR; Luo W
    Neurosci Lett; 2010 Jun; 477(1):19-22. PubMed ID: 20399249
    [TBL] [Abstract][Full Text] [Related]  

  • 25. [A new point mutation on exon 2 of parkin gene in Parkinson's disease].
    Xu Y; Liu Z; Wang Y; Tao E; Chen G; Chen B
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2002 Oct; 19(5):409-11. PubMed ID: 12362318
    [TBL] [Abstract][Full Text] [Related]  

  • 26. PINK1, Parkin, and DJ-1 mutations in Italian patients with early-onset parkinsonism.
    Klein C; Djarmati A; Hedrich K; Schäfer N; Scaglione C; Marchese R; Kock N; Schüle B; Hiller A; Lohnau T; Winkler S; Wiegers K; Hering R; Bauer P; Riess O; Abbruzzese G; Martinelli P; Pramstaller PP
    Eur J Hum Genet; 2005 Sep; 13(9):1086-93. PubMed ID: 15970950
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Analysis of the parkin deletion in sporadic and familial Parkinson's disease. Short communication.
    Krüger R; Vieira-Säcker AM; Kuhn W; Müller T; Woitalla D; Schöls L; Przuntek H; Epplen JT; Riess O
    J Neural Transm (Vienna); 1999; 106(2):159-63. PubMed ID: 10226936
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Analysis of PARK genes in a Korean cohort of early-onset Parkinson disease.
    Choi JM; Woo MS; Ma HI; Kang SY; Sung YH; Yong SW; Chung SJ; Kim JS; Shin HW; Lyoo CH; Lee PH; Baik JS; Kim SJ; Park MY; Sohn YH; Kim JH; Kim JW; Lee MS; Lee MC; Kim DH; Kim YJ
    Neurogenetics; 2008 Oct; 9(4):263-9. PubMed ID: 18704525
    [TBL] [Abstract][Full Text] [Related]  

  • 29. [Preliminary studies on parkin gene deletion at exons 1 to 6 in Chinese patients with praecox Parkinson's disease].
    Bia H; Shao M; Dong X; Yang J; Gao Q; Li Y; Chen B
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2000 Oct; 17(5):323-5. PubMed ID: 11024210
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Effective quantitative real-time polymerase chain reaction analysis of the parkin gene (PARK2) exon 1-12 dosage.
    Shadrina MI; Semenova EV; Slominsky PA; Bagyeva GH; Illarioshkin SN; Ivanova-Smolenskaia II; Limborska SA
    BMC Med Genet; 2007 Feb; 8():6. PubMed ID: 17324265
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Mutation screening and association analysis of the parkin gene in Parkinson's disease patients from South-West China.
    Peng R; Gou Y; Yuan Q; Li T; Latsoudis H; Yuan G; Luo D; Liu X; Collier DA
    Eur Neurol; 2003; 49(2):85-9. PubMed ID: 12584415
    [TBL] [Abstract][Full Text] [Related]  

  • 32. [Exon rearrangement analysis of parkin gene in patients with isolated early-onset parkinsonism using semi-quantitative PCR].
    Guo JF; Tang BS; Li J; Zhang YH; Zhang XW; Chen T; Xia K; Yan XX; Cao L; Cai F; Pan Q; Shen L; Jiang H
    Zhonghua Yi Xue Za Zhi; 2006 Jun; 86(21):1447-9. PubMed ID: 16842693
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Analysis of PARK2 gene exon rearrangements in Russian patients with sporadic Parkinson's disease.
    Semenova EV; Shadrina MI; Slominsky PA; Ivanova-Smolenskaya IA; Bagyeva G; Illarioshkin SN; Limborska SA
    Mov Disord; 2012 Jan; 27(1):139-42. PubMed ID: 21915905
    [TBL] [Abstract][Full Text] [Related]  

  • 34. The importance of gene dosage studies: mutational analysis of the parkin gene in early-onset parkinsonism.
    Hedrich K; Kann M; Lanthaler AJ; Dalski A; Eskelson C; Landt O; Schwinger E; Vieregge P; Lang AE; Breakefield XO; Ozelius LJ; Pramstaller PP; Klein C
    Hum Mol Genet; 2001 Aug; 10(16):1649-56. PubMed ID: 11487568
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Defining the ends of Parkin exon 4 deletions in two different families with Parkinson's disease.
    Clarimon J; Johnson J; Dogu O; Horta W; Khan N; Lees AJ; Hardy J; Singleton A
    Am J Med Genet B Neuropsychiatr Genet; 2005 Feb; 133B(1):120-3. PubMed ID: 15635662
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Parkin and PINK1 mutations in early-onset Parkinson's disease: comprehensive screening in publicly available cases and control.
    Brooks J; Ding J; Simon-Sanchez J; Paisan-Ruiz C; Singleton AB; Scholz SW
    J Med Genet; 2009 Jun; 46(6):375-81. PubMed ID: 19351622
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Distribution, type, and origin of Parkin mutations: review and case studies.
    Hedrich K; Eskelson C; Wilmot B; Marder K; Harris J; Garrels J; Meija-Santana H; Vieregge P; Jacobs H; Bressman SB; Lang AE; Kann M; Abbruzzese G; Martinelli P; Schwinger E; Ozelius LJ; Pramstaller PP; Klein C; Kramer P
    Mov Disord; 2004 Oct; 19(10):1146-57. PubMed ID: 15390068
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Parkin mutations and susceptibility alleles in late-onset Parkinson's disease.
    Oliveira SA; Scott WK; Martin ER; Nance MA; Watts RL; Hubble JP; Koller WC; Pahwa R; Stern MB; Hiner BC; Ondo WG; Allen FH; Scott BL; Goetz CG; Small GW; Mastaglia F; Stajich JM; Zhang F; Booze MW; Winn MP; Middleton LT; Haines JL; Pericak-Vance MA; Vance JM
    Ann Neurol; 2003 May; 53(5):624-9. PubMed ID: 12730996
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Differential expression of splice variant and wild-type parkin in sporadic Parkinson's disease.
    Tan EK; Shen H; Tan JM; Lim KL; Fook-Chong S; Hu WP; Paterson MC; Chandran VR; Yew K; Tan C; Yuen Y; Pavanni R; Wong MC; Puvan K; Zhao Y
    Neurogenetics; 2005 Dec; 6(4):179-84. PubMed ID: 16086186
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Influence of heterozygosity for parkin mutation on onset age in familial Parkinson disease: the GenePD study.
    Sun M; Latourelle JC; Wooten GF; Lew MF; Klein C; Shill HA; Golbe LI; Mark MH; Racette BA; Perlmutter JS; Parsian A; Guttman M; Nicholson G; Xu G; Wilk JB; Saint-Hilaire MH; DeStefano AL; Prakash R; Williamson S; Suchowersky O; Labelle N; Growdon JH; Singer C; Watts RL; Goldwurm S; Pezzoli G; Baker KB; Pramstaller PP; Burn DJ; Chinnery PF; Sherman S; Vieregge P; Litvan I; Gillis T; MacDonald ME; Myers RH; Gusella JF
    Arch Neurol; 2006 Jun; 63(6):826-32. PubMed ID: 16769863
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.